Variant #0000675622 (NC_000001.10:g.21044177A>G, NM_020816.2:c.23T>C (KIF17))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.21044177A>G
DNA change (hg38) -
Published as KIF17(NM_020816.3):c.23T>C (p.V8A)
ISCN -
DB-ID KIF17_000003
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 9.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SH2D5 NM_001103160.1 ?/. - c.*4108T>C r.(=) p.(=)
KIF17 NM_020816.2 ?/. - c.23T>C r.(?) p.(Val8Ala)


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